It was about 15 years ago when we embarked on our exciting journey to establish a Jewish educational network in Glen Waverly, Australia. We were about a 30-minute drive from the main Jewish neighborhood, and it was quite a challenge for a young and seemingly inexperienced couple with two small children.

Soon after we moved, a woman began coming to a playgroup I had started. She had one little boy and was expecting another child soon. You can't imagine the smile on her face when she told me she was pregnant with twins. Unfortunately, toward the end of her pregnancy, she no longer felt movement. Tragically, she gave birth to stillborn twin girls. Their grief was unimaginable.

What does she know about life's challenges?

This young devastated couple, came to spend Yom Kippur with us so that they could walk to shul on this holiest day. We spoke and I shared some thoughts from Chassidus (chassidic teaching) about dealing with tragedy and about G-d and His mysterious ways. But all along, I felt that perhaps I had no right to speak. In my mind, I kept thinking that she was probably wondering, "What would she know? Here she is, young, with two healthy children--what does she know about life's challenges?"

Yet I spoke from the heart and tried to be there for her. This fear, however, lingered in my mind. How could we speak to couples and offer counseling to people with much more life experience then we had? How could our words penetrate the hearts of others who went through what we would never want to experience?

And then our son Baruch was born.

My third pregnancy began like my others, with the excitement of knowing we were bringing another child into this world. Yet as time went on, I began feeling unwell. I seemed to be much larger than in my previous pregnancies, and I would often get dizzy spells and sudden periods of intense hunger. My obstetrician kept assuring me that all was normal, but in my heart, I did not think so.

Two weeks before my scheduled c-section, my waters broke and we went immediately to the hospital. It was not long before the doctor arrived and I was prepped for surgery.

When I awoke, the first thing I wanted to know was what I had, a boy or girl. The nurses would not say. They kept saying, "The doctor will come in soon." This avoidance of the question made me quite panicky and I remember crying out to them, "Why won't you tell me? Is the baby ok? What is wrong?"

The doctor finally came and told me that all was not well. The baby had some problems and was being transferred as we spoke to the newborn intensive care unit of one of the major hospitals. The ambulance officers brought the baby in the humidicrib and all I could see was tubes and more tubes... and then they took him away. It was a few days before I was strong enough to go to the other hospital to see him.

He had a cleft lip and palate and his esophagus was not fully formed. This condition, known as Tracheal Esophageal Fistula, was repairable, the nurse informed me, as were his cleft lip and palate. A few surgeries and he would be just fine, was their prediction.

We named him early on, since we knew it would be some time before he would have a brit. The name Baruch Refael (which means "Blessed is the One who heals") seemed most appropriate, for we knew that only G-d would be the one to heal him. This seemed especially appropriate for the Hebrew month of Iyar in which he was born, since the name Iyar is an acronym for Ani Hashem Rofecha--"I am G-d who heals you."

A whirlwind of surgeries

At three days old, our son underwent his first surgery. Thus began a seven-month-long stay in the intensive care unit. It was not as easy as they first predicted. Yes, they fixed the esophagus at three days and his cleft lip at three weeks, but he was unable to nurse and even the use of a bottle with a special attachment for cleft palates did not help. He would just get distressed and breathless, and he would often stop breathing and turn blue.

Finally, at five months, the doctors decided that something else might be happening. Scans of his heart showed an abnormal valve that needed to be opened. Complications with this heart procedure then led to open-heart surgery which, while successful, revealed that he also had a hole in his heart.

It was then that we discovered that our son had CHARGE syndrome. CHARGE is an acronym for an abnormal pattern of birth defects that appear in one out of every 9,000-10,000 births. The diagnosis led to a hearing test, since ear abnormalities and/or deafness is common. We then found out that our son was profoundly deaf in both ears.

Because of his problems swallowing, he underwent surgery for a gastrostomy to insert a tube in his stomach for feeding. When this wasn't successful, he needed a tracheostomy, a tube through his neck. The care of a tracheostomy was quite daunting, and it was a few weeks before we were confident enough to look after him ourselves.

Those first seven months of Baruch's life seemed like a lifetime. I spent all day, every day, at the hospital. I was pumping, so that Baruch would have breast milk for as long as possible. Looking back, I don't know how I did it, but I kept this up for months. My other two children, ages 2 and 3.5 when Baruch was born, were in preschool. I would leave the house after my husband left to take them to school and I would try to be home by the time they returned.

My life was a blur and most of my friends did not know what to say, so they did not say anything. It was very isolating, yet I was also perhaps not ready to share too much at that point either. A biweekly session with the social worker at the hospital was quite helpful. Not knowing all the problems at once probably helped as well. We focused on one issue at a time, since it was always "just one more hurdle" to overcome.

We scheduled his brit to take place in the hospital before he went home. The mohel came and we had a small family affair. The next week, at the age of seven and a half months, Baruch Refael finally came home, but he needed 24-hour care. He could not be left alone at all, since every few minutes, his tube needed to be cleared for him to breathe.

We had no idea what the ramifications of full-time care meant, but fortunately, a friend of mine did. She took matters into her own hands and raised the necessary funds so that we could afford a live-in "nanny" to help with his care. I had the night duty, since I could at least catch some sleep during the day. My husband had to leave early each morning for work to support us, but he was a tremendous help with our other two young children, not to mention that he handled all the cooking. (Fortunately, this has continued until today!)

Baruch needed constant care for two years, until he was finally old enough and strong enough to cough up his secretions, eliminating the need to be suctioned every five minutes!

Learning from Chassidus

Interestingly, Baruch was born in the month of Iyar, which is the middle of the school year here in Australia. Just that year I had begun to teach Chassidus in addition to the Bible, Prophets, and Judaic classes that I had already been teaching for a few years at the girls' high school. We had just finished the topic of Divine Providence and dealing with tests and challenges, when I was given my own personal challenge.

One of my first thoughts was that G-d had sent me the ability to heal before He presented me with the problem. Teaching something allows the subject matter to be internalized in a way that cannot happen if you just learn it for yourself. It was the teaching of Chassidus that helped me through those months, and many a time, I said, ashreinu mah tov chelkeinu--"how fortunate arewe, how good is our lot." I don't know how I would have made sense or found meaning in our situation without the Torah.

One of the first people I thought of when pondering our challenges, was this young woman who had lost her twins. I wanted to tell her, "Everything I told you then, I still believe! I have not changed one thing even though I am now faced with this tremendous challenge myself." (I did see her a few months later and a new relationship was forged. Since then, we have been fortunate to celebrate together the births of two more children for her, and for us as well.)

It’s in G-d’s Hands

Just when we thought we were over the biggest hurdle, at one year, when Baruch Rafael was back in the hospital for a cleft palate repair, he caught a virus. He got high fever, suffered muscle damage, went into kidney failure, and then was put on a respirator.

I was sitting with a cousin of mine as the doctor told me that Baruch’s heart was definitely affected, and he would probably die over the weekend. I remember looking at the doctor and thinking: "You are not G-d. That is your opinion, but anything can happen." My lack of verbal response to the doctor was unnerving for him. He kept asking me if I had understood what he said.

We prepared ourselves for the worst and I remember getting phone calls from people around the world telling us that they were reciting Psalms for our son. But, I also remember so vividly that I did not pray for him to recover. Rather, I prayed for G-d to give me the strength to go on, no matter what He decided. If He wanted to take my son from me, then I asked for the strength to cope with that. And if He chose to let my son recover from this situation, then I asked for the strength to continue caring for him, for we did not know in what state he would be in.

Miraculously, his kidneys did kick back in and he was weaned off the respirator. We took him home as a "vegetable." He had lost the ability to move, to sit and even to smile--all the things he had been doing before we entered the hospital for his palate repair. It took a week before he smiled again, a few weeks for him to begin rolling over and a few years before he was again able to sit unaided.

Moving Forward

Baruch began walking with the aid of a walker to walk at about the age of 4 or 5 and continued to depend on one until he was around 9. Now, he walks independently, although with a very distinct gait. He wears a helmet at all times to protect his head in case of a fall. We communicate entirely in sign language, and he attends a special school.

Unfortunately, the tracheostomy never did come out, which severely limits our options for care or respite. There are also the challenges of trying to do the best for him as well as for the rest of the family (he has four siblings, two older and two younger), in addition to our outreach work.

Baruch Refael HaCohen is turning 13 this Iyar, but he functions more on the level of a 6-8 year old then his true age. How to mark his Bar Mitzvah is a dilemma that we are working through right now.

But believing that one definitely has the ability to cope is the most important factor in actually coping with day-to-day challenges. I often think how fortunate we truly are for so many things, and most importantly, that we have a Torah that assures us that G-d does not give us any challenges that we cannot overcome--not necessarily completely on our own, but it is within our grasp. Reaching out to the right supports is, to me, a corollary to this concept.

I also continue to be grateful that we have Chassidus, which helps us to see this world through a different set of glasses. Special children are just that, "special" souls sent to this world for a very specific mission. When we open our eyes, we begin to see the positive affects they have on the people around them, ourselves included.

It has been 12 years since the doctor told me that my baby wouldn't live. And contrary to what we were told, he didn't remain a "vegetable." Baruch Refael is a very happy child and whoever meets him cannot help but be positively affected by him. He has given us all a deeper understanding of life, and the ability to reach out to others in a way that others can't. He has touched many lives while he has completely changed ours.

Whether it is the outpouring of goodwill and lovingkindness, the saying of Psalms, the learning of patience, or a plain and simple appreciation of life that we often take for granted, they are a constant reminder that there is a G-d in this world who works in ways that we do not always understand. Yet, He is there, sending us His messages through our lives. It is merely up to us to unravel them.

I wrote this poem shortly after Baruch Refael's birth:

The Waves of Life

Ride the waves of life, my friend
Some high, some fierce, some with no end
But you'll not be washed away by them
If you can ride the waves of life, my friend
Weights may try to pull you down
Emotions full of pain
But hold on to a board
And ride the waves, my friend
A board will keep you up above
The water deep and mean
And let you ride the waves of life
Ride the waves with ease
And what's the board, this heaven-sent
To hold onto in the sea?
This board, my friend, is nothing new
You had it all along with you
But you have to know it's there before
You can use its strength to hold and more
The board, my friend, is nothing new
It's just the strength of the inner you
So ride the waves of life, my friend
Ride the waves with ease
Let the water splash your face
Like grass sprinkled with dew
For you can still keep the pace
If you hold onto the strength of the real you
And ride the waves of life

Sara Rosenfeld is Chabad emissary in Melbourne, Australia. Reprinted with permission from chabad.org, Judaism and Jewish info. on the web.

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